# Major Recall Alert: Baxter Corporation Recalls Reusable Blood Pressure Cuffs Due to Latex Contamination in Packaging
Baxter Corporation has issued an urgent voluntary recall of several reusable blood pressure cuffs. Although the products are labeled “not made with natural rubber latex,” a latex-containing rubber band has been identified around the product's *Instructions for Use (IFU)*. This discrepancy has raised concerns for individuals with latex allergies who may inadvertently come into contact with the material.
The recall officially began on **March 20, 2025** and applies to unopened, affected products that remain in their original packaging. If you own or use any of the listed blood pressure cuffs, it’s vital to follow Baxter Corporation’s recall instructions immediately.
## Why This Recall is Important
Latex allergies can cause mild to severe reactions in certain individuals. Those who are sensitive to latex may experience symptoms like itching, skin irritation, hives, respiratory issues, or, in extreme cases, anaphylaxis. Baxter Corporation is recalling these blood pressure cuffs out of an abundance of caution to prevent potential harm.
While the cuffs themselves do not contain latex, the issue lies with a tiny rubber band containing natural latex that is included in the product’s packaging. Medical professionals, caregivers, and consumers are strongly advised to take all necessary precautions by identifying and returning affected products.
## Details of the Recall
Here’s a summary of the recall details:
### **Products Affected**
- **Brand**: Blood Pressure Cuff – Adult – Nylon, and related products
- **Affected Models**:
- **Connect Integrated Wall System (CIWS)**:
- 850000 Wireless
- 840000 Standard
- Connex Spot Monitor Series:
- 7300, 7400, and 7500
- Blood Pressure Cuffs:
- Adult, Child, Infant, Large Adult, Newborn, Thigh
- GS 777 Int'D Diag Sys W/Panop/Stp
- Vital Signs Monitor 6000 Series:
- CVSM 6700 and CVSM 6800
- Vital Signs Monitor Core
- Welch Allyn Spot Vital Signs 4400
### **Recall Reason**
- An unexpected **latex-containing rubber band** was discovered around the packaging’s *Instructions for Use (IFU)* despite labels stating the product was “not made with natural rubber latex.” This creates a risk for people with latex sensitivity or allergies.
### **Initiation Date**: March 20, 2025
### **Safety Measures**
- Affected blood pressure cuffs should not be used.
- Only unopened products in their packaging are eligible for return.
For additional details, visit the official recall announcement at [recalls-rappels.canada.ca](https://recalls-rappels.canada.ca/en/alert-recall/baxter-corporation-reusable-blood-pressure-cuffs).
## What You Should Do
If you are currently using or storing any of the recalled blood pressure cuffs, follow these steps:
1. **Check the product packaging**: Review the model number, brand, and series to see if it matches any of the recall details above.
2. **Stop using the product**: Avoid using the blood pressure cuff, especially if you or someone under your care has a latex sensitivity.
3. **Return unopened products**: Baxter Corporation is requesting the return of all unopened, affected cuffs still in their packaging. Contact Baxter or follow instructions from the official recall notice.
4. **Spread the word**: Inform colleagues, caregivers, or medical practices about this recall to minimize risk.
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For more details about this recall, including specific product identifiers and next steps, visit the official [Baxter Blood Pressure Cuff Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/baxter-corporation-reusable-blood-pressure-cuffs). Stay informed, stay safe!